Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_assertion description "[CSF GAP-43 levels were analysed in benign intracranial hypertension, movement disorders, multiple sclerosis, neuropathy, CNS infections, motor neuron disease, and headache (neurological controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_assertion evidence source_evidence_literature NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_assertion SIO_000772 25175067 NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_assertion wasDerivedFrom befree-20150227 NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_assertion wasGeneratedBy ECO_0000203 NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418000.RAl7-Xmy8dY_s3BURIB6UzpgLyx_MpkpevjzEODPBLP18130_provenance.